SLMAP Antikörper

Produktnummer ABIN6293579

Produktdetails anti-SLMAP Antikörper

Target: SLMAP (Sarcolemma Associated Protein (SLMAP))

Reaktivität: Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser SLMAP Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Aufreinigung: Affinity purification

Immunogen: Recombinant protein of human SLMAP

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB 1:500 - 1:2000

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Buffer: PBS with 0.02 % sodium azide, 50 % glycerol,  pH 7.3.

Konservierungsmittel: Sodium azide

Vorsichtsmaßnahmen: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Lagerung: -20 °C

Informationen zur Lagerung: Store at -20C. Avoid freeze / thaw cycles.

Details zu SLMAP

Target: SLMAP (Sarcolemma Associated Protein (SLMAP))

Andere Bezeichnung: SLMAP (SLMAP Produkte)

Synonyme: SLAP antikoerper, D330001L02Rik antikoerper, Slap antikoerper, mKIAA1601 antikoerper, MGC55817 antikoerper, zgc:55817 antikoerper, SLMAP antikoerper, fa03e05 antikoerper, fb39b03 antikoerper, wu:fa03e05 antikoerper, wu:fb39b03 antikoerper, zgc:153887 antikoerper, sarcolemma associated protein antikoerper, sarcolemma associated protein b antikoerper, sarcolemmal membrane-associated protein antikoerper, sarcolemma associated protein a antikoerper, SLMAP antikoerper, Slmap antikoerper, slmapb antikoerper, slmap antikoerper, LOC100435366 antikoerper, slmapa antikoerper

Hintergrund: This gene encodes a component of a conserved striatin-interacting phosphatase and kinase complex. Striatin family complexes participate in a variety of cellular processes including signaling, cell cycle control, cell migration, Golgi assembly, and apoptosis. The protein encoded by this gene is a coiled-coil, tail-anchored membrane protein with a single C-terminal transmembrane domain that is posttranslationally inserted into membranes. Mutations in this gene are associated with Brugada syndrome, a cardiac channelopathy. Alternative splicing results in multiple transcript variants.

Molekulargewicht: 95.198 kDa

Gen-ID: 7871

UniProt: Q14BN4